Changes of the body composition, physical performances and serum metabolite profile among novice male adolescent field hockey players: the implication of genetic and strength training intensity / Elin Elisa Khairul
Studies suggested that genes are one of the contributing factors that affect an athlete’s performance, aside from a well-designed training programme. Therefore, training response following different strength training (ST) intensity in individuals with different genotypes profile needs to be explored...
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| Format: | Thesis |
| Language: | English |
| Published: |
2023
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| Online Access: | https://ir.uitm.edu.my/id/eprint/88881/1/88881.pdf |
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| Summary: | Studies suggested that genes are one of the contributing factors that affect an athlete’s performance, aside from a well-designed training programme. Therefore, training response following different strength training (ST) intensity in individuals with different genotypes profile needs to be explored. This study aimed to investigate the changes in body composition (skeletal muscle mass [SMM], body fat percentage [BF%]), physical performances (upper [UBS] and lower body strength [LBS], lower body power [LBP], percentage of sprint decrement [%Sdec], maximal oxygen uptake [VO2max]), and serum metabolites profile following different ST intensity and genotypes profile. A total of 45 male adolescent field hockey players (age=16.5±0.5 years old, height=1.60±0.5 m, weight=61.0±6.7 kg) were randomly assigned into; 1) high intensity [H] ST (3 sets of 6 repetitions at 80 to 90% 1RM), 2) moderate intensity [M] ST (3 sets of 8 repetitions at 60 to 75% 1RM) and a control group (C) whom did not take part in any ST sessions. Six selected upper and lower body exercise routines were prescribed three times per week for eight weeks, non-consecutively. Pre- (week 0) and post-training (week 9) measures of body composition and physical performances were determined. Participants were genotyped for nine gene polymorphisms; strength-power and endurance: ACE (rs1799752), ACTN3 (rs1815739), PPARA (rs4253778), strength-power: AGT (rs699), TRHR (rs7832552), endurance: ADRB3 (rs4994), BDKRB2 (rs1799722), PPARGC1A (rs8192678), and VEGFA (rs2010963). Subsequently, global metabolomics analysis (liquid chromatography-mass spectrometry) was conducted on 15 participants. The effect of different ST intensities on the changes of body composition and physical performances were examined through one-way analysis of variance (ANOVA). The effect of different genotype profiles and ST intensities on body composition and physical performance changes were examined through a mixed between-within ANOVA. The metabolomics data were analysed using Mass Profiler Professional software and MetaboAnalyst 5.0. The H group shown significantly greater improvement compared to M and C in the body composition (SMM: H=28.80±3.47 to 29.70±3.32 kg, M=27.83±2.89 to 28.21±2.91 kg, C=27.56±2.27 to 27.60±2.26 kg; BF%: H=13.42±2.99 to 12.42±3.03 %, M=15.45±4.39 to 15.02±4.43 %, C=13.04±3.47 to 13.97±3.38 %) and physical performances (UBS: H=44.93±3.84 to 66.80±4.28 kg, M=44.13±3.81 to 60.40±4.73 kg, C=44.13±3.81 to 43.87±4.10 kg; LBS: H= 123.00±11.62 to 165.60±15.77 kg, M=122.33±13.21 to 140.87±10.90 kg, C=118.47±9.08 to 114.00±10.72 kg; LBP: H=4.27±.61 to 5.06±.57 kW, M=3.58±.72 to 4.03±.73 kW, C=3.79±.51 to 3.68±.50 kW; %Sdec: H=8.75±1.92 to 7.04±1.82 %, M=9.56±2.35 to 9.23±2.32 %, C=9.25±2.38 to 9.80±2.85 %) except for VO2max, post-training. The polymorphisms of ACE (rs1799752) and BDKRB2 (rs1799722) exerted significant interaction effect upon LBS, F(4,36)=4.94, p<.05, ηp2=0.35 and UBS, F(4,36)=6.21, p<.05, ηp2=0.41, respectively. Two metabolites (3-O-Sulfogalactoslyceramide, Sphingosine-1-phosphate) significantly differ between training groups and were chosen as the potential biomarkers following ST. In conclusion, prescribing HST resulted in greater body composition and physical performances changes. Moreover, combination of favourable genetic profiles with appropriate training intensity is advantageous to novice adolescent athletes. Finally, metabolome changes offer the identification of metabolite signature following ST. |
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